Using the marine rotifer Brachionus plicatilis acute toxicity tests, we estimated the toxicity of Corexit 9500A®, propylene glycol, and Macondo oil. Ratios of 1:10, 1:50 and 1:130 for Corexit 9500A®:Macondo oil mixture represent: maximum exposure concentrations, recommended ratios for deploying Corexit (1:10–1:50), 1:130 the actual dispersant:oil ratio used in the Deep Water Horizon spill. Corexit 9500A® and oil are similar in their toxicity. However, when Corexit 9500A® and oil are mixed, toxicity to B. manjavacas increases up to 52-fold. Extrapolating these results to the oil released by the Macondo well, suggests underestimation of increased toxicity from Corexit application. We found small differences in sensitivity among species of the B. plicatilis species complex, likely reflecting phylogenetic similarity. Just 2.6% of the water-accommodated fraction of oil inhibited rotifer cyst hatching by 50%, an ecologically significant result because rotifer cyst in sediments are critical resources for the recolonization of populations each Spring.

We investigated how additions of choline, a naturally occurring methylated nitrogen-containing compound, accelerated hydrocarbon degradation in sandy sediments contaminated with moderately weathered crude oil (4000 mg kg−1 sediment). Addition of lauroylcholine chloride (LCC) and tricholine citrate (TCC) to oil contaminated sediments resulted in 1.6 times higher hydrocarbon degradation rates compared to treatments without added choline derivatives. However, the degradation rate constant for the oil contaminated sediments amended with LCC was similar to that in contaminated sediments amended with inorganic nitrogen, phosphorus, and glucose. Additions of LLC and TCC to sediments containing extensively weathered oil also resulted in enhanced mineralization rates. Cultivation-free 16S rRNA analysis revealed the presence of an extant microbial community with clones closely related to known hydrocarbon degraders from the Gammaproteobacteria, Alphaproteobacteria, and Firmicutes phyla. The results demonstrate that the addition of minimal amounts of organic compounds to oil contaminated sediments enhances the degradation of hydrocarbons.

Phytotoxicity results are reviewed for oils, dispersants and dispersed oils. The phytotoxicity database consists largely of results from a patchwork of reactive research conducted after oil spills to marine waters. Toxicity information is available for at least 41 crude oils and 56 dispersants. As many as 107 response parameters have been monitored for 85 species of unicellular and multicellular algae, 28 wetland plants, 13 mangroves and 9 seagrasses. Effect concentrations have varied by as much as six orders of magnitude due to experimental diversity. This diversity restricts phytotoxicity predictions and identification of sensitive species, life stages and response parameters. As a result, evidence-based risk assessments for most aquatic plants and petrochemicals and dispersants are not supported by the current toxicity database. A proactive and experimentally-consistent approach is recommended to provide threshold toxic effect concentrations for sensitive life stages of aquatic plants inhabiting diverse ecosystems.

Crude oil is a complex mixture of petroleum hydrocarbons (PHC) with distinct chemical, physical and toxicological properties relevant for contaminated site risk assessment. Ecotoxicological effects of crude oil distillation fractions on luminescent bacteria (Vibrio fischeri), earthworms (Dendrobaena hortensis) and invertebrates (Heterocypris incongruens) were tested using two spiked soils and their elutriates. Fraction 2 (F2) had an equivalent carbon number (ECN) range of >10 to 16, and F3 from >16 to 39. F2 showed a substantially higher ecotoxicological effect than F3 for Vibrio and Dendrobaena. In contrast, severe inhibition of Heterocypris by the poorly soluble F3 is attributed to mechanical organ blockage. Immediate sequestration of PHC to the organic matter-rich soil effected reduced toxicity for all organisms. This study indicates that a more differentiated consideration (i) of PHC mixtures based on ECN range and (ii) of model soil properties employed for ecotoxicity testing should be included into PHC-contaminated site risk assessment.

A consortium composed of many different bacterial species is required to efficiently degrade polycyclic aromatic hydrocarbons (PAH) in oil-contaminated soil. We obtained six PAH-degrading microbial consortia from three oil-contaminated soils using two different isolation culture media. Denaturing gradient gel electrophoresis (DGGE) and sequence analyses of amplified 16s rRNA genes confirmed the bacterial community was greatly affected by both the culture medium and the soil from which the consortia were enriched. Three bacterial consortia enriched using malt yeast extract (MYE) medium showed higher degradation rates of PAHs than consortia enriched using Luria broth (LB) medium. Consortia obtained from a soil and then added back to that same soil was more effective in degrading PAHs than adding, to the same soil, consortia isolated from other, unrelated soils. This suggests that inoculum used for bioremediation should be from the same, or very similar nearby soils, as the soil that is actually being bioremediated.

We tested the hypothesis that the biodegradation of volatile petroleum hydrocarbons (VPHs) in aerobic sandy soil is affected by the blending with 10 percent ethanol (E10) or 20 percent biodiesel (B20). When inorganic nutrients were scarce, competition between biofuel and VPH degraders temporarily slowed monoaromatic hydrocarbon degradation. Ethanol had a bigger impact than biodiesel, reflecting the relative ease of ethanol compared to methyl ester biodegradation. Denaturing gradient gel electrophoresis (DGGE) of bacterial 16S rRNA genes revealed that each fuel mixture selected for a distinct bacterial community, each dominated by Pseudomonas spp. Despite lasting impacts on soil bacterial ecology, the overall effects on VHP biodegradation were minor, and average biomass yields were comparable between fuel types, ranging from 0.40 ± 0.16 to 0.51 ± 0.22 g of biomass carbon per gram of fuel carbon degraded. Inorganic nutrient availability had a greater impact on petroleum hydrocarbon biodegradation than fuel composition.

Recently, several researchers have attempted to address Deepwater Horizon incident environmental fate and effects issues using laboratory testing and extrapolation procedures that are not fully reliable measures for environmental assessments. The 2013 Rico-Martínez et al. publication utilized laboratory testing approaches that severely limit our ability to reliably extrapolate such results to meaningful real-world assessments.The authors did not adopt key methodological elements of oil and dispersed oil toxicity standards. Further, they drew real-world conclusions from static exposure tests without reporting actual exposure concentrations. Without this information, it is not possible to compare their results to other research or real spill events that measured and reported exposure concentrations.The 1990s' Chemical Response to Oil Spills: Ecological Effects Research Forum program was established to standardize and conduct exposure characterization in oil and dispersed oil aquatic toxicity testing (Aurand and Coelho, 2005). This commentary raises awareness regarding the necessity of standardized test protocols.

Pipeline systems used to transport petroleum products represent a potential source of soil pollution worldwide. The design of new techniques that may improve current monitoring of pipeline leakage is imperative. This paper assesses the remote detection of small leakages of liquid hydrocarbons indirectly, through the analysis of spectral features of contaminated plants. Leaf and canopy spectra of healthy plants were compared to spectra of plants contaminated with diesel and gasoline, at increasing rates of soil contamination. Contamination effects were observed both visually in the field and thorough changes in the spectral reflectance patterns of vegetation. Results indicate that the remote detection of small volumes of gasoline and diesel contaminations is feasible based on the red edge analysis of leaf and canopy spectra of plants. Brachiaria grass ranks as a favourable choice to be used as an indicator of HCs leakages along pipelines.

1H NMR metabolomics and conventional ecotoxicity endpoints were used to examine the response of earthworms exposed to petroleum hydrocarbons (PHCs) in soil samples collected from a site that was contaminated with crude oil from a pipeline failure in the mid-1990s. The conventional ecotoxicity tests showed that the soils were not acutely toxic to earthworms (average survival ≥90%), but some soil samples impaired reproduction endpoints by >50% compared to the field control soil. Additionally, metabolomics revealed significant relationships between earthworm metabolic profiles (collected after 2 or 14 days of exposure) and soil properties including soil PHC concentration. Further comparisons by partial least squares regression revealed a significant relationship between the earthworm metabolomic data (collected after only 2 or 14 days) and the reproduction endpoints (measured after 63 days). Therefore, metabolomic responses measured after short exposure periods may be predictive of chronic, ecologically relevant toxicity endpoints for earthworms exposed to soil contaminants.

Airborne exposures of carcinogenic and co–carcinogenic pollutants, emitted from industries and various diffuse sources in a 10km radius of Gibraltar, were calculated at the west side of the Rock of Gibraltar facing the Bay. 2005 and 2008 industrial annual emission rates reported to E–PRTR and 2005 municipal diffuse annual emission rates were entered in OML–Multi, a multi–source version of an atmospheric Gaussian plume local scale dispersion model. The model results reveal that carcinogens PAH, represented by benzo[a]pyrene (BaP), arsenic and nickel, and potentially chromium are the priority pollutants with respect to human cancer risk and that the contribution from industrial sources on the Spanish coastal area exceeds that from the diffuse sources from adjacent Spanish municipalities. There is a decrease in annual mean air concentrations from industrial emissions between the years 2005 and 2008. The assessment of contribution to the Gibraltar air concentrations of the priority pollutants from industrial sources shows that refinery CEPSA, chemical industry Petresa and petroleum industry Lubricantes del Sur are significant for nickel. Chemical industry Interquisa is significant for PAHs with a notable decrease in PAH emissions from 2006 to 2007, whereas the contribution from CEPSA is more constant. For arsenic only CEPSA shows a continuous trend and contributes to the 2008 air concentration together with sewerage Edar de la Linea de la Concepcion. CEPSA and metal industry Acerinox contribute the most to the chromium air concentrations. NO2/NOx is the most critical co–carcinogen and electricity plant Central Termica Los Barrios, CEPSA, electricity plant Generacion Electrica Peninsular and electricity plant Cogeneracion de Interquisa are the most significant contributors to the air concentrations in Gibraltar. Pollutant contributions from CEPSA flaring, ship traffic in the Bay and Strait, local road traffic and local diesel generators are currently un–quantified.